Background During the dilute acid pretreatment process, the resulting pseudo-lignin and lignin droplets deposited on the surface of lignocellulose and inhibit the enzymatic digestibility of cellulose in lignocellulose. However, how these lignins interact with cellulase enzymes and then affect enzymatic hydrolysis is still unknown. In this work, different fractions of surface lignin (SL) obtained from dilute acid-pretreated bamboo residues (DAP-BR) were extracted by various organic reagents and the residual lignin in extracted DAP-BR was obtained by the milled wood lignin (MWL) method. All of the lignin fractions obtained from DAP-BR were used to investigate the mechanism for interaction between lignin and cellulase using surface plasmon resonance (SPR) technology to understand how they affect enzymatic hydrolysis Results The results showed that removing surface lignin significantly decreased the yield for enzymatic hydrolysis DAP-BR from 36.5% to 18.6%. The addition of MWL samples to Avicel inhibited its enzymatic hydrolysis, while different SL samples showed slight increases in enzymatic digestibility. Due to the higher molecular weight and hydrophobicity of MWL samples versus SL samples, a stronger affinity for MWL (KD = 6.8–24.7 nM) was found versus that of SL (KD = 39.4–52.6 nM) by SPR analysis. The affinity constants of all tested lignins exhibited good correlations (r > 0.6) with the effects on enzymatic digestibility of extracted DAP-BR and Avicel. Conclusions This work revealed that the surface lignin on DAP-BR is necessary for maintaining enzyme digestibility levels, and its removal has a negative impact on substrate digestibility.

Lignin nano-particles (LNPs) exhibit properties that distinguish them from the production of other lignin-based materials. However, little research has been performed to investigate whether porous carbons produced from LNPs exhibit a performance superior to those derived from untreated lignin. In this study, lignin was fabricated into LNPs and used to prepare high-performance porous carbons with enhanced thermal conductivities compared to that of carbons from neat lignin. Two different preparation protocols were employed: direct pyrolysis and hydrothermal carbonization followed by pyrolysis. Carbons obtained from 100 to 300 nm LNPs possessed more graphene-like structures than carbons from unaltered lignin. In addition, carbons prepared using a combination of hydrothermal carbonization and pyrolysis exhibited higher specific surface areas (108.81-220.75 m 2 /g) and total pore volumes (0.098-0.166 cm 3 /g) than those prepared via direct pyrolysis. In addition, LNP-derived carbons exhibited superior thermal conductivities (0.45 W/mK) and thermal conductivity rates (0.51 • C/s). This work provides the useful finding that superior graphene-like porous carbons can be produced by transforming lignin into LNP and then hydrothermally carbonizing the resulting material prior to pyrolysis.

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The isolongifolanone derivative (2c) exhibit highly selective and sensitive fluorescence quenching towards copper ions, and this was used for real-time sensing of cooper ions in vivo.

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Three ketene nopinone derivatives (1–3) were successfully synthesized from β-pinene derivative nopinone.